Buspirone Hydrochloride
- Product NDC
- 50090-7161
- 11-digit product format
- 500907161
- Labeler code
- 50090
- Product ID
- 50090-7161_13dc568c-6efc-4bfb-835a-c0e86059f1b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210907
- Marketing category
- ANDA
- Marketing start
- 2023-10-17
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Buspirone Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUSPIRONE HYDROCHLORIDE | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 207LT9J9OC |
| Rxcui | 866018 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-7161-1 | Buspirone Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 6 |
| 50090-7161-3 | Buspirone Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7161 | BUSPIRONE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 6 | Current NDC, 2 package rows | 20240511_2a25a718-306f-403e-9928-cae30bc52f12.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7161-1 | 50090716101 | 60 TABLET in 1 BOTTLE (50090-7161-1) | 60 tablet | 2024-05-06 | No | No | Current |
| 50090-7161-3 | 50090716103 | 90 TABLET in 1 BOTTLE (50090-7161-3) | 90 tablet | 2024-05-06 | No | No | Current |